Doxylamine Succinate and Pyridoxine HCl Delayed Tablets Recall
The FDA is recalling Doxylamine Succinate and Pyridoxine HCl Delayed-Release tablets 10 mg/10 mg, 100-count bottles distributed nationwide. The recall is due to the presence of foreign tablets/capsules. The affected lot is DMA25006 with expiration 11/30/2028; NDC 69452-206-20, involving 14,232 bottles (1,423,200 tablets).
| Brand | Bionpharma Inc. |
|---|---|
| Product | Doxylamine Succinate and Pyridoxine HCl Delayed-Release tablets 10 mg/10 mg, 100-count bottle, Rx Only, MADE IN INDIA, Distributed by: Bionpharma Inc., Princeton, NJ 08540 NDC 69452-206-20. |
| Reason | Presence of Foreign Tablets/Capsules |
| Severity | low |
| Units affected | 14232 |
| Distribution | US Nationwide. |
| Agency | FDA |
WHAT YOU SHOULD DO
- Do not use any affected product.
- Check if your bottle belongs to lot DMA25006 and expires 11/30/2028; set it aside if it does.
- Contact your pharmacist or healthcare provider for guidance and potential replacement or refund.
- Return or dispose of the affected product according to local guidelines or the purchasing outlet.
How to identify the recalled item
| Lot / date codes | Lot # DMA25006, Exp Date: 11/30/2028. |
|---|---|
| Lot / date codes | Lot # DMA25006, Exp Date: 11/30/2028. |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
Other Bionpharma Inc. recalls
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.